I.S. EN 60601-2-41:2009
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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MEDICAL ELECTRICAL EQUIPMENT - PART 2-41: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF SURGICAL LUMINAIRES AND LUMINAIRES FOR DIAGNOSIS
Hardcopy, PDF
20-12-2021
01-01-2009
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FOREWORD
INTRODUCTION
201.1 Scope, object and related standards
201.2 Normative references
201.3 Terms and definitions
201.4 General requirements
201.5 General requirements for testing of ME EQUIPMENT
201.6 Classification of ME EQUIPMENT and ME SYSTEMS
201.7 ME EQUIPMENT Identification, marking and documents
201.8 Protection against electrical HAZARDS from ME
EQUIPMENT
201.9 Protection against mechanical hazards of ME
EQUIPMENT and ME SYSTEMS
201.10 Protection against unwanted and excessive
radiation HAZARDS
201.11 Protection against excessive temperatures and
other HAZARDS
201.12 Accuracy of controls and instruments and protection
against hazardous outputs
201.13 HAZARDOUS SITUATIONS and fault conditions
201.14 PROGRAMMABLE ELECTRICAL MEDICAL SYSTEMS (PEMS)
201.15 Construction of ME EQUIPMENT
201.16 ME SYSTEMS
201.17 Electromagnetic compatibility of ME EQUIPMENT and
ME SYSTEMS
Annex AA (informative) - Guidance and rationale for
particular clauses and subclauses
Bibliography
Index of defined terms
Annex ZA (normative) - Normative references to international
publications with their corresponding European
publications
Annex ZZ (informative) - Coverage of Essential Requirements
of EC Directives
Pertains to the BASIC SAFETY and ESSENTIAL PERFORMANCE of SURGICAL LUMINAIRES AND LUMINAIRES FOR DIAGNOSIS, hereafter referred to as ME EQUIPMENT.
| DevelopmentNote |
For CENELEC adoptions of IEC publications, please check www.iec.ch to be sure that you have any corrigenda that may apply. (01/2017)
|
| DocumentType |
Standard
|
| Pages |
51
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Superseded
|
| SupersededBy |
| Standards | Relationship |
| UNE-EN 60601-2-41:2010 | Identical |
| DIN EN 60601-2-41 : 2016 | Identical |
| BS EN 60601-2-41 : 2009 | Identical |
| SN EN 60601-2-41 : 2009 AMD 11 2011 | Identical |
| NF EN 60601-2-41 : 2010 AMD 1 2015 | Identical |
| EN 60601-2-41:2009/A1:2015 | Identical |
| ISO 9680:2014 | Dentistry Operating lights |
| IEC 60601-2-50:2009+AMD1:2016 CSV | Medical electrical equipment - Part 2-50: Particular requirementsfor the basic safety and essential performance of infant phototherapy equipment |
| IEC 60601-2-18:2009 | Medical electrical equipment - Part 2-18: Particular requirements for the basic safety and essential performance of endoscopic equipment |
| ISO 11664-1:2007 | Colorimetry Part 1: CIE standard colorimetric observers |
| EN 60598-2-9:1989/A1:1994 | Luminaires - Part 2: Particular requirements - Section 9: Photo and film luminaires (non-professional) |
| IEC 60598-2-25:1994 | Luminaires - Part 2: Particular requirements - Section 25: Luminaires for use in clinical areas of hospitals and health care buildings |
| IEC 60598-1:2014+AMD1:2017 CSV | Luminaires - Part 1: General requirements and tests |
| IEC 60598-2-22:2014+AMD1:2017 CSV | Luminaires - Part 2-22: Particular requirements - Luminaires for emergency lighting |
| IEC 60598-2-4:2017 | Luminaires - Part 2-4: Particular requirements - Portable general purpose luminaires |
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